Variant report

Variant	rs55920669
Chromosome Location	chr12:21854335-21854336
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:21853672..21855818-chr12:22198436..22200574,2	K562	blood:

Variant related genes	Relation type
ENSG00000111726	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs16924221	1.00[AMR][1000 genomes]
rs1813751	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2081819	1.00[AMR][1000 genomes]
rs2217238	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55713096	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56013787	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56035640	1.00[AMR][1000 genomes]
rs56055068	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56066637	1.00[AMR][1000 genomes]
rs56160727	1.00[AMR][1000 genomes]
rs56871137	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57115374	1.00[AMR][1000 genomes]
rs57338327	1.00[AMR][1000 genomes]
rs58998049	1.00[AMR][1000 genomes]
rs59046730	1.00[AMR][1000 genomes]
rs59468844	1.00[AMR][1000 genomes]
rs60462646	1.00[AMR][1000 genomes]
rs60632805	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61187969	1.00[AMR][1000 genomes]
rs61482461	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7133951	1.00[AMR][1000 genomes]
rs7136997	1.00[AMR][1000 genomes]
rs74067603	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74067604	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74067606	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74067608	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74067609	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74067610	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74067611	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74069345	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74069349	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74069350	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74069351	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74069353	1.00[AMR][1000 genomes]
rs74069355	1.00[AMR][1000 genomes]
rs74069356	1.00[AMR][1000 genomes]
rs74069357	1.00[AMR][1000 genomes]
rs74069365	1.00[AMR][1000 genomes]
rs74069366	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043936	chr12:21562673-21979030	ZNF genes & repeats Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
2	nsv557741	chr12:21578559-22169854	Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv469164	chr12:21688900-21966701	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv557744	chr12:21688900-21966701	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv832349	chr12:21749093-21930695	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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